Cell therapy as a strategy to minimize maintenance immunosuppression in solid organ transplant recipients

被引:29
作者
Geissler, Edward K. [1 ]
Hutchinson, James A. [1 ]
机构
[1] Univ Hosp Regensburg, Dept Surg, Regensburg, Germany
关键词
cell therapy; Mreg; Treg; The One Study; Tol-DC; Tr1; REGULATORY T-CELLS; MESENCHYMAL STEM-CELLS; TOLEROGENIC DENDRITIC CELLS; CARDIAC ALLOGRAFT SURVIVAL; ACCEPTANCE-INDUCING-CELLS; SUPPRESSOR-CELL; COSTIMULATORY BLOCKADE; FOXP3; EXPRESSION; EXPANSION; TOLERANCE;
D O I
10.1097/MOT.0b013e328363319d
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Purpose of reviewThis review presents a clinically focussed introduction to cell-based immunotherapy in solid organ transplantation. The potential benefits and risks of cell-based immunotherapeutics are critically discussed.Recent findingsThe use of immunoregulatory cells as medicinal agents is very much in its infancy, but the field is expanding rapidly. In principle, this approach permits manipulation of specific immunological functions, opening new possibilities in the field of tolerance-promoting therapies. Several immunoregulatory cell types have reached the point of preclinical and clinical development that should allow them to be tested in early-phase clinical trials. Solid organ transplantation represents an important potential indication for the use of cell-based immunosuppressive agents because promoting immunological regulation towards allografts remains a promising strategy for preventing chronic rejection.SummaryRemarkable progress is being made in the implementation of novel cell-based immunotherapeutics in solid organ transplantation studies. It is hoped that these new immunoregulatory therapies will afford better long-term transplant outcomes by mitigating chronic graft injury.
引用
收藏
页码:408 / 415
页数:8
相关论文
共 62 条
[1]   Human tolerogenic DC-10: perspectives for clinical applications [J].
Amodio, Giada ;
Gregori, Silvia .
TRANSPLANTATION RESEARCH, 2012, 1
[2]   Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells [J].
Battaglia, M ;
Stabilini, A ;
Roncarolo, MG .
BLOOD, 2005, 105 (12) :4743-4748
[3]   Outcome of alloanergized haploidentical bone marrow transplantation after ex vivo costimulatory blockade: results of 2 phase 1 studies [J].
Davies, Jeff K. ;
Gribben, John G. ;
Brennan, Lisa L. ;
Yuk, Dongin ;
Nadler, Lee M. ;
Guinan, Eva C. .
BLOOD, 2008, 112 (06) :2232-2241
[4]   Costimulatory blockade with monoclonal antibodies to induce alloanergy in donor lymphocytes [J].
Davies, Jeffrey K. .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2011, 93 (05) :594-601
[5]  
Davies JK, 2012, CELL TRANSPLANT
[6]  
Davies JK, 2011, J VIS EXP, P49
[7]   Immunomagnetic isolation of CD4+CD25+FoxP3+ natural T regulatory lymphocytes for clinical applications [J].
Di Ianni, M. ;
Del Papa, B. ;
Cecchini, D. ;
Bonifacio, E. ;
Moretti, L. ;
Zei, T. ;
Ostini, R. Iacucci ;
Falzetti, F. ;
Fontana, L. ;
Tagliapietra, G. ;
Maldini, C. ;
Martelli, M. F. ;
Tabilio, A. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2009, 156 (02) :246-253
[8]   Regulatory T cells in stem cell transplantation: strategies and first clinical experiences [J].
Edinger, Matthias ;
Hoffmann, Petra .
CURRENT OPINION IN IMMUNOLOGY, 2011, 23 (05) :679-684
[9]   Mesenchymal stem cell-educated macrophages [J].
Eggenhofer, Elke ;
Hoogduijn, Martin J. .
TRANSPLANTATION RESEARCH, 2012, 1
[10]  
Geissler EK, 2012, TRANSPLANT RES, V1, DOI [10.1186/2047-1440-1-10, 10.1186/2047-1440-1-11]